HU201230B - Acaricides with synergetic effect and comprising thiophosphoryl glycineamide derivative as active ingredient - Google Patents

Acaricides with synergetic effect and comprising thiophosphoryl glycineamide derivative as active ingredient Download PDF

Info

Publication number: HU201230B
Authority: HU; Hungary
Prior art keywords: weight; ethyl; alkyl; propyl; compound
Prior art date: 1987-11-17

Application number

HU874645A

Other languages

German (de)

English (en)

Hungarian (hu)

Other versions

HUT48104A (en

Inventor

Laszlone Bartha

Zsolt Dombay

Karoly Balogh

Jozsef Nagy

Gyula Tarpai

Karoly Fodor

Janosne Magyar

Erzsebet Mile

Gaborne Pipoly

Karoly Pasztor

Gusztavne Szabo

Laszlone Urszin

Original Assignee

Eszakmagyar Vegyimuevek

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1987-11-17

Filing date

1987-11-17

Publication date

1990-10-28

1987-11-17 Application filed by Eszakmagyar Vegyimuevek filed Critical Eszakmagyar Vegyimuevek

1987-11-17 Priority to HU874645A priority Critical patent/HU201230B/hu

1988-10-26 Priority to SK7085-88A priority patent/SK278148B6/sk

1988-10-26 Priority to CS887085A priority patent/CZ278704B6/cs

1988-10-27 Priority to US07/416,312 priority patent/US4993332A/en

1988-10-27 Priority to UA4614604A priority patent/UA19066A/uk

1988-10-27 Priority to AT0901488A priority patent/AT400072B/de

1988-10-27 Priority to GB8916131A priority patent/GB2239697B/en

1988-10-27 Priority to DD88321139A priority patent/DD276519A1/de

1988-10-27 Priority to PCT/HU1988/000070 priority patent/WO1989004940A1/de

1989-05-29 Publication of HUT48104A publication Critical patent/HUT48104A/hu

1989-07-14 Priority to SU894614604A priority patent/SU1732821A3/ru

1990-10-28 Publication of HU201230B publication Critical patent/HU201230B/hu

1993-08-30 Priority to LTRP906A priority patent/LT2297B/xx

Links

-1 thiophosphoryl glycineamide derivative Chemical class 0.000 title claims description 96
239000004480 active ingredient Substances 0.000 title claims description 40
230000000895 acaricidal effect Effects 0.000 title claims description 27
230000002195 synergetic effect Effects 0.000 title claims description 8
239000000642 acaricide Substances 0.000 title description 6
239000000203 mixture Substances 0.000 claims description 67
LWLJUMBEZJHXHV-UHFFFAOYSA-N Dienochlor Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C1(Cl)C1(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LWLJUMBEZJHXHV-UHFFFAOYSA-N 0.000 claims description 31
FOANIXZHAMJWOI-UHFFFAOYSA-N bromopropylate Chemical compound C=1C=C(Br)C=CC=1C(O)(C(=O)OC(C)C)C1=CC=C(Br)C=C1 FOANIXZHAMJWOI-UHFFFAOYSA-N 0.000 claims description 30
239000003995 emulsifying agent Substances 0.000 claims description 26
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 21
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 16
239000000843 powder Substances 0.000 claims description 16
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 10
239000000080 wetting agent Substances 0.000 claims description 10
125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 8
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 claims description 8
239000002270 dispersing agent Substances 0.000 claims description 8
125000000217 alkyl group Chemical group 0.000 claims description 6
239000007788 liquid Substances 0.000 claims description 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
239000007787 solid Substances 0.000 claims description 6
239000005909 Kieselgur Substances 0.000 claims description 5
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 4
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 4
239000011575 calcium Substances 0.000 claims description 4
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 4
239000000945 filler Substances 0.000 claims description 4
BEBCJVAWIBVWNZ-UHFFFAOYSA-N glycinamide Chemical class NCC(N)=O BEBCJVAWIBVWNZ-UHFFFAOYSA-N 0.000 claims description 4
229910052736 halogen Inorganic materials 0.000 claims description 4
ZRYCRPNCXLQHPN-UHFFFAOYSA-N 3-hydroxy-2-methylbenzaldehyde Chemical compound CC1=C(O)C=CC=C1C=O ZRYCRPNCXLQHPN-UHFFFAOYSA-N 0.000 claims description 3
125000003545 alkoxy group Chemical group 0.000 claims description 3
229910052791 calcium Inorganic materials 0.000 claims description 3
235000014113 dietary fatty acids Nutrition 0.000 claims description 3
239000000194 fatty acid Substances 0.000 claims description 3
229930195729 fatty acid Natural products 0.000 claims description 3
150000004665 fatty acids Chemical class 0.000 claims description 3
125000005843 halogen group Chemical group 0.000 claims description 3
150000002367 halogens Chemical class 0.000 claims description 3
150000004760 silicates Chemical class 0.000 claims description 3
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 2
125000001931 aliphatic group Chemical group 0.000 claims description 2
150000001408 amides Chemical class 0.000 claims description 2
125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 claims description 2
239000000454 talc Substances 0.000 claims description 2
229910052623 talc Inorganic materials 0.000 claims description 2
125000004953 trihalomethyl group Chemical group 0.000 claims description 2
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
239000004215 Carbon black (E152) Substances 0.000 claims 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
235000019738 Limestone Nutrition 0.000 claims 1
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims 1
125000003118 aryl group Chemical group 0.000 claims 1
CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical group C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 claims 1
229930195733 hydrocarbon Natural products 0.000 claims 1
150000002430 hydrocarbons Chemical class 0.000 claims 1
239000006028 limestone Substances 0.000 claims 1
238000000034 method Methods 0.000 abstract description 6
239000003245 coal Substances 0.000 abstract 10
238000002485 combustion reaction Methods 0.000 abstract 8
238000010304 firing Methods 0.000 abstract 3
238000010298 pulverizing process Methods 0.000 abstract 2
238000007664 blowing Methods 0.000 abstract 1
239000002817 coal dust Substances 0.000 abstract 1
238000005243 fluidization Methods 0.000 abstract 1
239000000446 fuel Substances 0.000 abstract 1
230000000630 rising effect Effects 0.000 abstract 1
150000001875 compounds Chemical class 0.000 description 73
239000012141 concentrate Substances 0.000 description 49
HDWLUGYOLUHEMN-UHFFFAOYSA-N Dinobuton Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)OC(C)C HDWLUGYOLUHEMN-UHFFFAOYSA-N 0.000 description 46
238000002360 preparation method Methods 0.000 description 38
231100000111 LD50 Toxicity 0.000 description 32
238000003756 stirring Methods 0.000 description 31
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 29
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 25
239000000839 emulsion Substances 0.000 description 25
238000009472 formulation Methods 0.000 description 25
239000008096 xylene Substances 0.000 description 25
231100000419 toxicity Toxicity 0.000 description 19
230000001988 toxicity Effects 0.000 description 19
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 17
229940125904 compound 1 Drugs 0.000 description 16
241000238876 Acari Species 0.000 description 14
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 14
239000004563 wettable powder Substances 0.000 description 14
239000003795 chemical substances by application Substances 0.000 description 12
238000005259 measurement Methods 0.000 description 12
241000239290 Araneae Species 0.000 description 11
241001454293 Tetranychus urticae Species 0.000 description 11
239000002904 solvent Substances 0.000 description 11
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
241000196324 Embryophyta Species 0.000 description 9
238000005507 spraying Methods 0.000 description 9
238000002474 experimental method Methods 0.000 description 8
244000141359 Malus pumila Species 0.000 description 7
238000011835 investigation Methods 0.000 description 7
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 7
239000000969 carrier Substances 0.000 description 6
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 6
235000011430 Malus pumila Nutrition 0.000 description 5
235000015103 Malus silvestris Nutrition 0.000 description 5
235000013399 edible fruits Nutrition 0.000 description 5
230000000694 effects Effects 0.000 description 5
239000005995 Aluminium silicate Substances 0.000 description 4
244000046052 Phaseolus vulgaris Species 0.000 description 4
239000013543 active substance Substances 0.000 description 4
235000012211 aluminium silicate Nutrition 0.000 description 4
229940125758 compound 15 Drugs 0.000 description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 4
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 4
239000004546 suspension concentrate Substances 0.000 description 4
GLGNXYJARSMNGJ-VKTIVEEGSA-N (1s,2s,3r,4r)-3-[[5-chloro-2-[(1-ethyl-6-methoxy-2-oxo-4,5-dihydro-3h-1-benzazepin-7-yl)amino]pyrimidin-4-yl]amino]bicyclo[2.2.1]hept-5-ene-2-carboxamide Chemical compound CCN1C(=O)CCCC2=C(OC)C(NC=3N=C(C(=CN=3)Cl)N[C@H]3[C@H]([C@@]4([H])C[C@@]3(C=C4)[H])C(N)=O)=CC=C21 GLGNXYJARSMNGJ-VKTIVEEGSA-N 0.000 description 3
IWZSHWBGHQBIML-ZGGLMWTQSA-N (3S,8S,10R,13S,14S,17S)-17-isoquinolin-7-yl-N,N,10,13-tetramethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-amine Chemical compound CN(C)[C@H]1CC[C@]2(C)C3CC[C@@]4(C)[C@@H](CC[C@@H]4c4ccc5ccncc5c4)[C@@H]3CC=C2C1 IWZSHWBGHQBIML-ZGGLMWTQSA-N 0.000 description 3
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 3
244000068988 Glycine max Species 0.000 description 3
235000010469 Glycine max Nutrition 0.000 description 3
239000003085 diluting agent Substances 0.000 description 3
238000011156 evaluation Methods 0.000 description 3
239000000243 solution Substances 0.000 description 3
125000001424 substituent group Chemical group 0.000 description 3
DRSHXJFUUPIBHX-UHFFFAOYSA-N COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 Chemical compound COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 DRSHXJFUUPIBHX-UHFFFAOYSA-N 0.000 description 2
229940126657 Compound 17 Drugs 0.000 description 2
235000008694 Humulus lupulus Nutrition 0.000 description 2
244000025221 Humulus lupulus Species 0.000 description 2
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
241000607479 Yersinia pestis Species 0.000 description 2
239000000654 additive Substances 0.000 description 2
235000021016 apples Nutrition 0.000 description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
XRWSZZJLZRKHHD-WVWIJVSJSA-N asunaprevir Chemical compound O=C([C@@H]1C[C@H](CN1C(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)(C)C)OC1=NC=C(C2=CC=C(Cl)C=C21)OC)N[C@]1(C(=O)NS(=O)(=O)C2CC2)C[C@H]1C=C XRWSZZJLZRKHHD-WVWIJVSJSA-N 0.000 description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
229940125810 compound 20 Drugs 0.000 description 2
229940126208 compound 22 Drugs 0.000 description 2
229940125961 compound 24 Drugs 0.000 description 2
229940126179 compound 72 Drugs 0.000 description 2
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
230000001804 emulsifying effect Effects 0.000 description 2
JAXFJECJQZDFJS-XHEPKHHKSA-N gtpl8555 Chemical compound OC(=O)C[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N[C@H](B1O[C@@]2(C)[C@H]3C[C@H](C3(C)C)C[C@H]2O1)CCC1=CC=C(F)C=C1 JAXFJECJQZDFJS-XHEPKHHKSA-N 0.000 description 2
150000008282 halocarbons Chemical class 0.000 description 2
238000000265 homogenisation Methods 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
239000002917 insecticide Substances 0.000 description 2
125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 2
239000011707 mineral Substances 0.000 description 2
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
239000000575 pesticide Substances 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
239000007921 spray Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
235000013311 vegetables Nutrition 0.000 description 2
NXSVXDCNLSWHME-FUBQLUNQSA-N (2S)-2-amino-N-(1-diphenoxyphosphorylethyl)-3-(1H-imidazol-5-yl)propanamide Chemical compound C([C@H](N)C(=O)NC(C)P(=O)(OC=1C=CC=CC=1)OC=1C=CC=CC=1)C1=CN=CN1 NXSVXDCNLSWHME-FUBQLUNQSA-N 0.000 description 1
GHYOCDFICYLMRF-UTIIJYGPSA-N (2S,3R)-N-[(2S)-3-(cyclopenten-1-yl)-1-[(2R)-2-methyloxiran-2-yl]-1-oxopropan-2-yl]-3-hydroxy-3-(4-methoxyphenyl)-2-[[(2S)-2-[(2-morpholin-4-ylacetyl)amino]propanoyl]amino]propanamide Chemical compound C1(=CCCC1)C[C@@H](C(=O)[C@@]1(OC1)C)NC([C@H]([C@@H](C1=CC=C(C=C1)OC)O)NC([C@H](C)NC(CN1CCOCC1)=O)=O)=O GHYOCDFICYLMRF-UTIIJYGPSA-N 0.000 description 1
WWTBZEKOSBFBEM-SPWPXUSOSA-N (2s)-2-[[2-benzyl-3-[hydroxy-[(1r)-2-phenyl-1-(phenylmethoxycarbonylamino)ethyl]phosphoryl]propanoyl]amino]-3-(1h-indol-3-yl)propanoic acid Chemical compound N([C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)O)C(=O)C(CP(O)(=O)[C@H](CC=1C=CC=CC=1)NC(=O)OCC=1C=CC=CC=1)CC1=CC=CC=C1 WWTBZEKOSBFBEM-SPWPXUSOSA-N 0.000 description 1
HUWSZNZAROKDRZ-RRLWZMAJSA-N (3r,4r)-3-azaniumyl-5-[[(2s,3r)-1-[(2s)-2,3-dicarboxypyrrolidin-1-yl]-3-methyl-1-oxopentan-2-yl]amino]-5-oxo-4-sulfanylpentane-1-sulfonate Chemical compound OS(=O)(=O)CC[C@@H](N)[C@@H](S)C(=O)N[C@@H]([C@H](C)CC)C(=O)N1CCC(C(O)=O)[C@H]1C(O)=O HUWSZNZAROKDRZ-RRLWZMAJSA-N 0.000 description 1
DYZYOIDAZOCKGK-UHFFFAOYSA-N (4-bromophenyl) 2-hydroxyacetate Chemical compound OCC(=O)OC1=CC=C(Br)C=C1 DYZYOIDAZOCKGK-UHFFFAOYSA-N 0.000 description 1
125000006273 (C1-C3) alkyl group Chemical group 0.000 description 1
125000001376 1,2,4-triazolyl group Chemical group N1N=C(N=C1)* 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
UNILWMWFPHPYOR-KXEYIPSPSA-M 1-[6-[2-[3-[3-[3-[2-[2-[3-[[2-[2-[[(2r)-1-[[2-[[(2r)-1-[3-[2-[2-[3-[[2-(2-amino-2-oxoethoxy)acetyl]amino]propoxy]ethoxy]ethoxy]propylamino]-3-hydroxy-1-oxopropan-2-yl]amino]-2-oxoethyl]amino]-3-[(2r)-2,3-di(hexadecanoyloxy)propyl]sulfanyl-1-oxopropan-2-yl Chemical compound O=C1C(SCCC(=O)NCCCOCCOCCOCCCNC(=O)COCC(=O)N[C@@H](CSC[C@@H](COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC)C(=O)NCC(=O)N[C@H](CO)C(=O)NCCCOCCOCCOCCCNC(=O)COCC(N)=O)CC(=O)N1CCNC(=O)CCCCCN\1C2=CC=C(S([O-])(=O)=O)C=C2CC/1=C/C=C/C=C/C1=[N+](CC)C2=CC=C(S([O-])(=O)=O)C=C2C1 UNILWMWFPHPYOR-KXEYIPSPSA-M 0.000 description 1
WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
QBWKPGNFQQJGFY-QLFBSQMISA-N 3-[(1r)-1-[(2r,6s)-2,6-dimethylmorpholin-4-yl]ethyl]-n-[6-methyl-3-(1h-pyrazol-4-yl)imidazo[1,2-a]pyrazin-8-yl]-1,2-thiazol-5-amine Chemical compound N1([C@H](C)C2=NSC(NC=3C4=NC=C(N4C=C(C)N=3)C3=CNN=C3)=C2)C[C@H](C)O[C@H](C)C1 QBWKPGNFQQJGFY-QLFBSQMISA-N 0.000 description 1
241000489242 Amphitetranychus viennensis Species 0.000 description 1
241001124076 Aphididae Species 0.000 description 1
235000002566 Capsicum Nutrition 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
240000008067 Cucumis sativus Species 0.000 description 1
235000009849 Cucumis sativus Nutrition 0.000 description 1
240000006497 Dianthus caryophyllus Species 0.000 description 1
235000009355 Dianthus caryophyllus Nutrition 0.000 description 1
241000735332 Gerbera Species 0.000 description 1
241000238631 Hexapoda Species 0.000 description 1
235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
241000758706 Piperaceae Species 0.000 description 1
244000018633 Prunus armeniaca Species 0.000 description 1
235000009827 Prunus armeniaca Nutrition 0.000 description 1
241000220324 Pyrus Species 0.000 description 1
241000109329 Rosa xanthina Species 0.000 description 1
235000004789 Rosa xanthina Nutrition 0.000 description 1
240000003768 Solanum lycopersicum Species 0.000 description 1
241001454295 Tetranychidae Species 0.000 description 1
241000219094 Vitaceae Species 0.000 description 1
240000006365 Vitis vinifera Species 0.000 description 1
235000014787 Vitis vinifera Nutrition 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
LNUFLCYMSVYYNW-ZPJMAFJPSA-N [(2r,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[[(3s,5s,8r,9s,10s,13r,14s,17r)-10,13-dimethyl-17-[(2r)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxy]-4,5-disulfo Chemical compound O([C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1C[C@@H]2CC[C@H]3[C@@H]4CC[C@@H]([C@]4(CC[C@@H]3[C@@]2(C)CC1)C)[C@H](C)CCCC(C)C)[C@H]1O[C@H](COS(O)(=O)=O)[C@@H](OS(O)(=O)=O)[C@H](OS(O)(=O)=O)[C@H]1OS(O)(=O)=O LNUFLCYMSVYYNW-ZPJMAFJPSA-N 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000002671 adjuvant Substances 0.000 description 1
150000005215 alkyl ethers Chemical class 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical class [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
239000011324 bead Substances 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
239000004927 clay Substances 0.000 description 1
229910052570 clay Inorganic materials 0.000 description 1
229940125797 compound 12 Drugs 0.000 description 1
229940126086 compound 21 Drugs 0.000 description 1
229940125846 compound 25 Drugs 0.000 description 1
230000001186 cumulative effect Effects 0.000 description 1
FWFSEYBSWVRWGL-UHFFFAOYSA-N cyclohex-2-enone Chemical compound O=C1CCCC=C1 FWFSEYBSWVRWGL-UHFFFAOYSA-N 0.000 description 1
229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
239000000428 dust Substances 0.000 description 1
238000010410 dusting Methods 0.000 description 1
235000013601 eggs Nutrition 0.000 description 1
125000006232 ethoxy propyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 description 1
230000003631 expected effect Effects 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
244000037666 field crops Species 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
239000008187 granular material Substances 0.000 description 1
235000021021 grapes Nutrition 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
238000005286 illumination Methods 0.000 description 1
208000015181 infectious disease Diseases 0.000 description 1
235000009973 maize Nutrition 0.000 description 1
238000002156 mixing Methods 0.000 description 1
230000001459 mortal effect Effects 0.000 description 1
230000001069 nematicidal effect Effects 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
239000002420 orchard Substances 0.000 description 1
235000021017 pears Nutrition 0.000 description 1
125000001863 phosphorothioyl group Chemical group *P(*)(*)=S 0.000 description 1
239000005648 plant growth regulator Substances 0.000 description 1
235000021018 plums Nutrition 0.000 description 1
238000002203 pretreatment Methods 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
238000011160 research Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
239000004575 stone Substances 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000003826 tablet Substances 0.000 description 1
238000012360 testing method Methods 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23C—METHODS OR APPARATUS FOR COMBUSTION USING FLUID FUEL OR SOLID FUEL SUSPENDED IN A CARRIER GAS OR AIR
- F23C1/00—Combustion apparatus specially adapted for combustion of two or more kinds of fuel simultaneously or alternately, at least one kind of fuel being either a fluid fuel or a solid fuel suspended in a carrier gas or air
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23C—METHODS OR APPARATUS FOR COMBUSTION USING FLUID FUEL OR SOLID FUEL SUSPENDED IN A CARRIER GAS OR AIR
- F23C10/00—Fluidised bed combustion apparatus
- F23C10/002—Fluidised bed combustion apparatus for pulverulent solid fuel
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23C—METHODS OR APPARATUS FOR COMBUSTION USING FLUID FUEL OR SOLID FUEL SUSPENDED IN A CARRIER GAS OR AIR
- F23C6/00—Combustion apparatus characterised by the combination of two or more combustion chambers or combustion zones, e.g. for staged combustion
- F23C6/04—Combustion apparatus characterised by the combination of two or more combustion chambers or combustion zones, e.g. for staged combustion in series connection
- F23C6/045—Combustion apparatus characterised by the combination of two or more combustion chambers or combustion zones, e.g. for staged combustion in series connection with staged combustion in a single enclosure
- F23C6/047—Combustion apparatus characterised by the combination of two or more combustion chambers or combustion zones, e.g. for staged combustion in series connection with staged combustion in a single enclosure with fuel supply in stages
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23K—FEEDING FUEL TO COMBUSTION APPARATUS
- F23K1/00—Preparation of lump or pulverulent fuel in readiness for delivery to combustion apparatus
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23C—METHODS OR APPARATUS FOR COMBUSTION USING FLUID FUEL OR SOLID FUEL SUSPENDED IN A CARRIER GAS OR AIR
- F23C2201/00—Staged combustion
- F23C2201/10—Furnace staging
- F23C2201/101—Furnace staging in vertical direction, e.g. alternating lean and rich zones
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23C—METHODS OR APPARATUS FOR COMBUSTION USING FLUID FUEL OR SOLID FUEL SUSPENDED IN A CARRIER GAS OR AIR
- F23C2201/00—Staged combustion
- F23C2201/30—Staged fuel supply
- F23C2201/301—Staged fuel supply with different fuels in stages

Landscapes

Engineering & Computer Science (AREA)
Chemical & Material Sciences (AREA)
Combustion & Propulsion (AREA)
Mechanical Engineering (AREA)
General Engineering & Computer Science (AREA)
Fluidized-Bed Combustion And Resonant Combustion (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)

HU874645A 1987-11-17 1987-11-17 Acaricides with synergetic effect and comprising thiophosphoryl glycineamide derivative as active ingredient HU201230B (en)

Priority Applications (11)

Application Number	Priority Date	Filing Date	Title
HU874645A HU201230B (en)	1987-11-17	1987-11-17	Acaricides with synergetic effect and comprising thiophosphoryl glycineamide derivative as active ingredient
SK7085-88A SK278148B6 (en)	1987-11-17	1988-10-26	Method of mixed combustion of coal and device for realization of this method
CS887085A CZ278704B6 (en)	1987-11-17	1988-10-26	Process and apparatus for combined combustion of coal
AT0901488A AT400072B (de)	1987-11-17	1988-10-27	Hybrides wirbelbett-kohlenstaub-feuerungssystem und verfahren zur umstellung von vorhandenen kohlensstaubkesseln auf dieses system
UA4614604A UA19066A (uk)	1987-11-17	1988-10-27	Гібридhа система спалюваhhя вугілля та вугільhого пилу в псевдозріджувальhому шарі
US07/416,312 US4993332A (en)	1987-11-17	1988-10-27	Hybrid fluidized bed and pulverized coal combustion system and a process utilizing said system
GB8916131A GB2239697B (en)	1987-11-17	1988-10-27	Hybrid fluidized bed and pulverized coal combustion system and a process for converting existing oulverized coal-fired boilers to this system.
DD88321139A DD276519A1 (de)	1987-11-17	1988-10-27	Hybrides wirbelbett-kohlenstaub-feuerungssystem und verfahren zur durchfuehrung
PCT/HU1988/000070 WO1989004940A1 (fr)	1987-11-17	1988-10-27	Systeme hybride de chauffage a lit fluidise/charbon pulverise et procede d'adaptation a ce systeme de chaudieres au charbon pulverise existantes
SU894614604A SU1732821A3 (ru)	1987-11-17	1989-07-14	Гибридна система сжигани угл и угольной пыли в псевдоожиженном слое
LTRP906A LT2297B (lt)	1987-11-17	1993-08-30	Anglies arba anglies dulkiu pseudosuskystintame sluoksnyje sudeginimo hibridine sistema

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
HU874645A HU201230B (en)	1987-11-17	1987-11-17	Acaricides with synergetic effect and comprising thiophosphoryl glycineamide derivative as active ingredient

Publications (2)

Publication Number	Publication Date
HUT48104A HUT48104A (en)	1989-05-29
HU201230B true HU201230B (en)	1990-10-28

Family

ID=10968559

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
HU874645A HU201230B (en)	1987-11-17	1987-11-17	Acaricides with synergetic effect and comprising thiophosphoryl glycineamide derivative as active ingredient

Country Status (10)

Country	Link
US (1)	US4993332A (cs)
AT (1)	AT400072B (cs)
CZ (1)	CZ278704B6 (cs)
DD (1)	DD276519A1 (cs)
GB (1)	GB2239697B (cs)
HU (1)	HU201230B (cs)
SK (1)	SK278148B6 (cs)
SU (1)	SU1732821A3 (cs)
UA (1)	UA19066A (cs)
WO (1)	WO1989004940A1 (cs)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GR1001285B (el) *	1990-01-08	1993-07-30	Evt Energie & Verfahrenstech	Μεθοδος δια την μειωσιν της εκπομπης οξειδιων του αζωτου κατα την καυση καρβουνοσκονης για ατμοπαραγωγους με ξηρο απορροφητηρα σταχτης.
US5176513A (en) *	1990-12-04	1993-01-05	Georgia Tech Research Corporation	Pulse combustor apparatus
US5216981A (en) *	1991-01-22	1993-06-08	Advanced Fuel Research, Inc.	Coal-fired heating apparatus and method
US5193490A (en) *	1991-09-03	1993-03-16	The Babcock & Wilcox Company	Cyclonic mixing and combustion chamber for circulating fluidized bed boilers
SE470213B (sv) *	1992-03-30	1993-12-06	Nonox Eng Ab	Sätt och anordning för framställning av bränslen ur fasta kolhaltiga naturbränslen
US5243922A (en) *	1992-07-31	1993-09-14	Institute Of Gas Technology	Advanced staged combustion system for power generation from coal
US5394937A (en) *	1993-03-05	1995-03-07	Nieh; Sen	Vortex heat exchange method and device
US5535687A (en) *	1994-08-25	1996-07-16	Raytheon Engineers & Constructors	Circulating fluidized bed repowering to reduce Sox and Nox emissions from industrial and utility boilers
RU2067724C1 (ru) *	1994-12-29	1996-10-10	Малое государственное внедренческое предприятие "Политехэнерго"	Низкоэмиссионная вихревая топка
US5765488A (en) *	1996-02-13	1998-06-16	Foster Wheeler Energy Corporation	Cyclone furnace combustion system and method utilizing a coal burner
RU2107223C1 (ru)	1996-08-15	1998-03-20	МГВП "Политехэнерго"	Топка
US5829368A (en) *	1996-12-31	1998-11-03	Combustion Engineering, Inc.	Fuel and sorbent feed for circulating fluidized bed steam generator
TW419574B (en) *	1998-06-16	2001-01-21	Mitsubishi Heavy Ind Ltd	Operating method of flow-level incinerator and the incinerator
US6145454A (en) *	1999-11-30	2000-11-14	Duke Energy Corporation	Tangentially-fired furnace having reduced NOx emissions
US6244200B1 (en)	2000-06-12	2001-06-12	Institute Of Gas Technology	Low NOx pulverized solid fuel combustion process and apparatus
US7004089B2 (en) *	2001-05-11	2006-02-28	Kvaerner Power Oy	Combined fluidized bed and pulverized coal combustion method
DE10203440A1 (de) *	2002-01-28	2003-08-14	Heinz Klewinkel	Verfahren und Vorrichtung zur Beschickung von industriellen Feuerungsanlagen mit Sekundärbrennstoff
ITBO20030242A1 (it) *	2003-04-23	2004-10-24	Itea Spa	Procedimento ed impianto per il trattamento di materiali
RU2253801C1 (ru) *	2004-07-12	2005-06-10	Григорьев Константин Анатольевич	Вихревая топка
US20080066731A1 (en) *	2006-08-02	2008-03-20	Johnson Geoffrey W A	Biomass pellet fuel heating device, system and method
US8349036B2 (en) *	2010-01-06	2013-01-08	General Electric Company	Systems and method for heating and drying solid feedstock in a gasification system
CN102226530A (zh) *	2011-06-10	2011-10-26	华能吉林发电有限公司九台电厂	发电厂锅炉煤粉燃料点火方法
JP6393981B2 (ja) *	2012-12-26	2018-09-26	三菱マテリアル株式会社	流動仮焼炉
JP6187315B2 (ja) *	2014-02-28	2017-08-30	三菱マテリアル株式会社	流動仮焼炉
CN105864748A (zh) *	2016-04-19	2016-08-17	上海理工大学	链条锅炉复合燃烧系统
CN105823038B (zh) *	2016-05-12	2017-12-26	内蒙古京泰发电有限责任公司	循环流化床锅炉大比例掺烧煤泥输煤系统

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1592847A (en) *	1977-12-14	1981-07-08	Worsley & Co Ltd G P	Fluid-bed furnaces
GB1604998A (en) *	1978-05-31	1981-12-16	Deborah Fluidised Combustion	Disposal of waste products by combustion
GB1604999A (en) *	1978-05-31	1981-12-16	Deborah Fluidised Combustion	Boilers
SE434087B (sv) *	1981-02-19	1984-07-02	Stal Laval Turbin Ab	Anleggning for forbrenning av orent fast brensle i en brennkammare med en fluidiserad bedd
US4397248A (en) *	1981-05-26	1983-08-09	Combustion Engineering, Inc.	Coal beneficiation/combustion system
DE3130602C2 (de) *	1981-08-01	1987-03-19	Steag Ag, 4300 Essen	Verfahren und Feuerung zum Verbrennen von festem Brennstoff
US4438709A (en) *	1982-09-27	1984-03-27	Combustion Engineering, Inc.	System and method for firing coal having a significant mineral content
JPS59195012A (ja) *	1983-04-20	1984-11-06	Hitachi Ltd	燃焼制御方法
SU1193377A1 (ru) *	1984-07-02	1985-11-23	Всесоюзный Дважды Ордена Трудового Красного Знамени Теплотехнический Научно-Исследовательский Институт Им.Ф.Э.Дзержинского	Способ подготовки и сжигани твердого топлива
SU1206556A1 (ru) *	1984-07-13	1986-01-23	Всесоюзный Дважды Ордена Трудового Красного Знамени Теплотехнический Научно-Исследовательский Институт Им.Ф.Э.Дзержинского	Способ подготовки и сжигани твердого топлива в кип щем слое
DD231840B1 (de) *	1984-08-14	1989-07-05	Univ Dresden Tech	Kohlenstaubdampferzeuger zur verbrennung von rohbraunkohle
DD249081B1 (de) *	1986-05-14	1990-03-28	Heizwerkausruestungen Heidenau	Verfahren zur wirbelschichtfeuerung und grosswasserraumkessel

1987
- 1987-11-17 HU HU874645A patent/HU201230B/hu not_active IP Right Cessation
1988
- 1988-10-26 CZ CS887085A patent/CZ278704B6/cs unknown
- 1988-10-26 SK SK7085-88A patent/SK278148B6/sk unknown
- 1988-10-27 DD DD88321139A patent/DD276519A1/de not_active IP Right Cessation
- 1988-10-27 GB GB8916131A patent/GB2239697B/en not_active Expired - Fee Related
- 1988-10-27 AT AT0901488A patent/AT400072B/de not_active IP Right Cessation
- 1988-10-27 WO PCT/HU1988/000070 patent/WO1989004940A1/de not_active Ceased
- 1988-10-27 US US07/416,312 patent/US4993332A/en not_active Expired - Fee Related
- 1988-10-27 UA UA4614604A patent/UA19066A/uk unknown
1989
- 1989-07-14 SU SU894614604A patent/SU1732821A3/ru active

Also Published As

Publication number	Publication date
GB2239697B (en)	1992-07-08
CZ278704B6 (en)	1994-05-18
GB8916131D0 (en)	1989-09-20
UA19066A (uk)	1997-12-25
WO1989004940A1 (fr)	1989-06-01
HUT48104A (en)	1989-05-29
CS708588A3 (en)	1992-02-19
AT400072B (de)	1995-09-25
ATA901488A (de)	1995-01-15
US4993332A (en)	1991-02-19
GB2239697A (en)	1991-07-10
SU1732821A3 (ru)	1992-05-07
DD276519A1 (de)	1990-02-28
SK278148B6 (en)	1996-02-07

Legal Events

Date	Code	Title	Description
1992-05-28	HPC4	Succession in title of patentee	Owner name: INTERMED INTERMEDIEREKET ES NOEVENYVEDOESZEREKET G
1992-08-28	HMM4	Cancellation of final prot. due to non-payment of fee
1992-11-30	HNF4	Restoration of lapsed final prot.
1994-07-28	HMM4	Cancellation of final prot. due to non-payment of fee
1994-09-28	HNF4	Restoration of lapsed final prot.
1995-07-28	HMM4	Cancellation of final prot. due to non-payment of fee

Publication	Publication Date	Title
HU201230B (en)	1990-10-28	Acaricides with synergetic effect and comprising thiophosphoryl glycineamide derivative as active ingredient
EA001470B1 (ru)	2001-04-23	Синергетическая гербицидная композиция и способ борьбы с сорняками
RU2273993C9 (ru)	2007-07-10	Гербицидные средства и способ борьбы с сорняками
FR2609369A1 (fr)	1988-07-15	Produit synergetique et procede pour la lutte selective contre les mauvaises herbes dans le riz
JPH0228159A (ja)	1990-01-30	複素環式２―アルコキシフエノキシスルホニル尿素類、それらの製造方法およびそれらを含有する除草剤
DK156658B (da)	1989-09-18	Triazinsubstituerede phenylsulfonylurinstoffer, herbicidt middel indeholdende disse forbindelser og fremgangsmaade til bekaempelse af uoensket vegetation under anvendelse af forbindelserne
HUT62766A (en)	1993-06-28	Herbicidal and plant growth regulating compositions comprising pyridylsulfonylurea salts as active ingrdient and process for producing such compounds
EP0477808B1 (en)	1997-07-16	Herbicides
JP2004508294A (ja)	2004-03-18	除草剤
FI90188B (fi)	1993-09-30	Herbisidisiä o-karbometoksisulfonyylikarbamideja
JPS63115861A (ja)	1988-05-20	α−イミノカルボン酸アニリドを含有する除草剤ならびに新規なα−イミノカルボン酸アニリドおよびその製造方法
HU206592B (en)	1992-12-28	Herbicide and growth controlling compositions containing substituted sulfonyl-diamide derivatives as active components and process for producing the active components
HU202846B (en)	1991-04-29	Herbicidal and plant growth regulating compositions comprising alkyl- and alkenylsulfonylurea derivatives substituted by heterocyclic group and process for producing the active ingredients
JPH0720960B2 (ja)	1995-03-08	新規スルホニル尿素，および除草および／又は生長調節用組成物
KR100240568B1 (ko)	2000-03-02	상승작용을 가진 제초 조성물
US4509974A (en)	1985-04-09	S-n-Butyl-N,N-diisopropyl thiocarbamate as a selective herbicide in cotton
RU2027715C1 (ru)	1995-01-27	Производное пиридинсульфонамида, обладающее гербицидной активностью
JP3789558B2 (ja)	2006-06-28	水田用除草剤組成物
JPH06172102A (ja)	1994-06-21	選択的除草用組成物
JP3687934B2 (ja)	2005-08-24	水田用除草剤組成物
HU189919B (en)	1986-08-28	Herbicide containing new 2-methyl-4-isopropyl-2-pentenoil-anilide compounds as agent and process for the production of the agent
DE3739691A1 (de)	1989-06-08	Phosphorhaltige sulfonylharnstoffe
HU204662B (en)	1992-02-28	Herbicidal composition having synergetic effect and comprising n-(substituted phenyl)-tetrahydrophthalimide derivative and n-(substituted phenyl)-n',n'-dimethylurea derivative, as well as utilization of the composition for exterminating wheeds
KR810000852B1 (ko)	1981-08-10	신규 안식향산 아닐리드 유도체의 제조방법
JP2767128B2 (ja)	1998-06-18	除草剤組成物